510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K852154Substantially Equivalent

Ackrad Sialography Catheter

Ackrad Laboratories, Cranford NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K852154 is the FDA 510(k) clearance record for ACKRAD SIALOGRAPHY CATHETER, cleared for Ackrad Laboratories on . FDA records list 42 510(k) clearances for Ackrad Laboratories, from to . As of , FDA records show no recalls naming K852154.

Clearance record

Decision date
Received
(40 days to decision)
Review panel
Unknown
Applicant
Ackrad Laboratories 70 Jackson Dr., Cranford NJ
Third party review
No